Allelic association of sequence variants in the herpes virus entry mediator-B gene (PVRL2) with the severity of multiple sclerosis (Q45416078)

14 December 2017

Allelic association of sequence variants in the herpes virus entry mediator-B gene (PVRL2) with the severity of multiple sclerosis (English)

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14 December 2017

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J L Haines

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14 December 2017

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L F Barcellos

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14 December 2017

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J R Oksenberg

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14 December 2017

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S L Hauser

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Multiple Sclerosis Genetics Group

14 December 2017

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object named as

Multiple Sclerosis Genetics Group

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14 December 2017

S Schmidt

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14 December 2017

M A Pericak-Vance

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14 December 2017

S Sawcer

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14 December 2017

J Hart

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14 December 2017

J Sims

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14 December 2017

A M Prokop

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14 December 2017

J van der Walt

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C DeLoa

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R R Lincoln

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A Compston

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S G Gregory

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1 June 2006

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384-392

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https://scigraph.springernature.com/pub.10.1038/sj.gene.6364311

14 December 2017

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cites work

Natural history of multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

A genetic basis for familial aggregation in multiple sclerosis. Canadian Collaborative Study Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

A population-based study of multiple sclerosis in twins: update.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Identifying disease modifying genes in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Preliminary observations on APOE epsilon4 allele and progression of disability in multiple sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Association of the APOE epsilon4 allele with disease activity in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Apoliprotein E and multiple sclerosis: impact of the epsilon-4 allele on susceptibility, clinical type and progression rate

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Apolipoprotein E epsilon 4 is associated with rapid progression of multiple sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Apolipoprotein E genotype related differences in brain lesions of multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

APOE genotype is a major predictor of long-term progression of disability in MS

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Association of APOE polymorphisms with disease severity in MS is limited to women.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Accelerated evolution of brain atrophy and "black holes" in MS patients with APOE-epsilon 4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Transverse myelopathy, a rare complication of mixed connective tissue disease: comparison with SLE related transverse myelopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Apolipoprotein E (APOE) phenotype and APOE concentrations in multiple sclerosis and acute herpes zoster.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Apolipoprotein E genotype does not influence the progression of multiple sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Genotypes at the APOE and SCA2 loci do not predict the course of multiple sclerosis in patients of Portuguese origin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Chromosome 19 single-locus and multilocus haplotype associations with multiple sclerosis. Evidence of a new susceptibility locus in Caucasian and Chinese patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Apolipoprotein E controls the risk and age at onset of Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Expression of apolipoprotein E during nerve degeneration and regeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Apolipoprotein E and the CNS response to injury.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Lack of apolipoprotein-E exacerbates experimental allergic encephalomyelitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

The role of the polio virus receptor and the herpesvirus entry mediator B genes for the development of MS

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Structural features of nectin-2 (HveB) required for herpes simplex virus entry

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

The splicing machinery is a genetic modifier of disease severity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Single-nucleotide polymorphisms in NAGNAG acceptors are highly predictive for variations of alternative splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Latent herpes simplex virus infection of sensory neurons alters neuronal gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Immune control of herpes simplex virus during latency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Gamma interferon can block herpes simplex virus type 1 reactivation from latency, even in the presence of late gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

High susceptibility of a human oligodendroglial cell line to herpes simplex type 1 infection.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Oligodendrocytes from human donors differ in resistance to herpes simplex virus 1 (HSV-1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Plaque-associated expression of human herpesvirus 6 in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Rating neurologic impairment in multiple sclerosis: An expanded disability status scale (EDSS)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

SNPselector: a web tool for selecting SNPs for genetic association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Activation of NF-kappaB and c-jun transcription factors in multiple sclerosis lesions. Implications for oligodendrocyte pathology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Epidemiologic evidence for multiple sclerosis as an infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Exact tests for association between alleles at arbitrary numbers of loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Removing the sampling restrictions from family-based tests of association for a quantitative-trait locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

A general test of association for quantitative traits in nuclear families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Family-based tests for associating haplotypes with general phenotype data: application to asthma genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

The structure of haplotype blocks in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

Natural history of multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

7 January 2021

APOE epsilon2-4 and -491 polymorphisms are not associated with MS

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

7 January 2021

APOE genotypes and disease severity in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

7 January 2021

Polymorphisms of apolipoprotein E and Japanese patients with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

7 January 2021

Linkage and association analysis of chromosome 19q13 in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

7 January 2021

An Icelandic example of the impact of population structure on association studies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

7 January 2021

Diagnostic criteria for multiple sclerosis research involving multiply affected families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

7 January 2021

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

7 January 2021

Large scale screening of the mitochondrial DNA reveals no pathogenic mutations but a haplotype associated with multiple sclerosis in Caucasians

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

7 January 2021

Mitochondrial dysfunction plays a key role in progressive axonal loss in Multiple Sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

7 January 2021

Inhibitors in the NFκB cascade comprise prime candidate genes predisposing to multiple sclerosis, especially in selected combinations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

7 January 2021

NFkappaB and AP-1 DNA binding activity in patients with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

7 January 2021

Viruses and multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

7 January 2021

Viruses and multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364311

7 January 2021

Identifiers

DOI

10.1038/SJ.GENE.6364311

1 reference

Dimensions Publication ID

14 December 2017

0 references

1 reference